The DOI matches its Crossref record; 91 of the 91 references it cites were found in a registry or an index.
The heritability of human disease: estimation, uses and abuses.
Abstract
Relatives provide the basic material for the study of inheritance of human disease. However, the methodologies for the estimation of heritability and the interpretation of the results have been controversial. The debate arises from the plethora of methods used, the validity of the methodological assumptions and the inconsistent and sometimes erroneous genetic interpretations made. We will discuss how to estimate disease heritability, how to interpret it, how biases in heritability estimates arise and how heritability relates to other measures of familial disease aggregation.
Overview
Integrity signals
Registry
Cites
Statistics
Verification
Claims the paper makes
Claims other papers make about this one
Each is checked against this paper’s own text: does it say what the citing paper says it does?
In the citing paper
“In addition to providing exceptional statistical power, the study directly addresses the concern of lack of replication in research findings 31,32 replicating results across 5 countries and health systems.”
From Association of Genetic and Environmental Factors With Autism in a 5-Country Cohort (2019) · cites this paper as [32]
Citations
Cites
A new look at the statistical model identification
Akaike, H. (1974) · IEEE Transactions on Automatic Control · doi:10.1109/tac.1974.1100705 · Cited by 51,879
Introduction to Quantitative Genetics.
Edwards, A. W. F., & Falconer, D. S. (1982) · Biometrics · doi:10.2307/2529912 · Cited by 21,447
Finding the missing heritability of complex diseases
Manolio, T. A., Collins, F. S., Cox, N. J., Goldstein, D. B., Hindorff, L. A., Hunter, D. J., McCarthy, M. I., Ramos, E. M., Cardon, L. R., Chakravarti, A., et al. (2009) · Nature · doi:10.1038/nature08494 · Cited by 8,336
Nelder, J. A., & Wedderburn, R. W. M. (1972) · Journal of the Royal Statistical Society Series A (General) · doi:10.2307/2344614 · Cited by 7,703
Genetics and Analysis of Quantitative Traits
(2002) · Journal of Animal Breeding and Genetics · doi:10.1046/j.1439-0388.2002.00356.x · Cited by 6,176
Common polygenic variation contributes to risk of schizophrenia and bipolar disorder
The International Schizophrenia Consortium (2009) · Nature · doi:10.1038/nature08185 · Cited by 4,821
Common SNPs explain a large proportion of the heritability for human height
Yang, J., Benyamin, B., McEvoy, B. P., Gordon, S., Henders, A. K., Nyholt, D. R., Madden, P. A., Heath, A. C., Martin, N. G., Montgomery, G. W., et al. (2010) · Nature Genetics · doi:10.1038/ng.608 · Cited by 4,446
Lichtenstein, P., Holm, N. V., Verkasalo, P. K., Iliadou, A., Kaprio, J., Koskenvuo, M., Pukkala, E., Skytthe, A., & Hemminki, K. (2000) · New England Journal of Medicine · doi:10.1056/nejm200007133430201 · Cited by 4,114
Recovery of Inter-Block Information when Block Sizes are Unequal
Patterson, H. D., & Thompson, R. (1971) · Biometrika · doi:10.1093/biomet/58.3.545 · Cited by 4,073
Methodology for Genetic Studies of Twins and Families
Neale, M. C., & Cardon, L. R. (1992) · doi:10.1007/978-94-015-8018-2 · Cited by 4,005
Flagged first, then by citations
Research works printed but not linked: 1
- Trimble, B. K. An Empirical Simulation of Quasi-Continuous Inheritance Using Human Birthweight Data. Thesis, McGill Univ. (1971).
Cited by
Sorted by citations
Items 101–200 of 281
Yang, C., Li, C., Kranzler, H. R., Farrer, L. A., Zhao, H., & Gelernter, J. E. (2013) · Human Genetics · doi:10.1007/s00439-013-1399-8 · Cited by 19
Baillie, J. K., Bretherick, A. D., Haley, C., Clohisey, S., Gray, A., Neyton, L. P. A., Barrett, J. C., Stahl, E. A., Tenesa, A., Andersson, R., et al. (2018) · PLoS Computational Biology · doi:10.1371/journal.pcbi.1005934 · Cited by 17
Thapar, A., & Harold, G. T. (2014) · Journal of Child Psychology and Psychiatry · doi:10.1111/jcpp.12294 · Cited by 19
Sex differences in white adipose tissue expansion: emerging molecular mechanisms
Bond, S. T., Calkin, A. C., & Drew, B. G. (2021) · Clinical Science · doi:10.1042/cs20210086 · Cited by 18
The missing heritability in type 1 diabetes
Pang, H., Lin, J., Luo, S., Huang, G., Li, X., Xie, Z., & Zhou, Z. (2022) · Diabetes Obesity and Metabolism · doi:10.1111/dom.14777 · Cited by 19
Arbet, J., McGue, M. K., & Basu, S. (2020) · Statistics in Medicine · doi:10.1002/sim.8564 · Cited by 18
Che, W. I., Westerlind, H., Lundberg, I. E., Hellgren, K. E., Kuja‐Halkola, R., & Holmqvist, M. E. (2021) · Annals of the Rheumatic Diseases · doi:10.1136/annrheumdis-2021-219914 · Cited by 18
Use of a Genealogical Database Demonstrates Heritability of Pulmonary Fibrosis
Scholand, M. B., Coon, H. H., Wolff, R. K., & Cannon‐Albright, L. (2013) · Lung · doi:10.1007/s00408-013-9484-2 · Cited by 20
Greives, T. J., Dochtermann, N. A., & Stewart, E. C. (2016) · Hormones and Behavior · doi:10.1016/j.yhbeh.2016.11.015 · Cited by 18
Heritability: What's the point? What is it not for? A human genetics perspective
Robette, N., Génin, E., & Clerget‐Darpoux, F. (2022) · Genetica · doi:10.1007/s10709-022-00149-7 · Cited by 20
Identifying genetically driven clinical phenotypes using linear mixed models
Mosley, J. D., Witte, J. S., Larkin, E. K., Bastarache, L. A., Shaffer, C. M., Karnes, J. H., Stein, C. M., Phillips, E. J., Hebbring, S. J., Brilliant, M. H., et al. (2016) · Nature Communications · doi:10.1038/ncomms11433 · Cited by 16
Dascalu, J., Liu, M., Lycett, K., Grobler, A. C., He, M., Burgner, D. P., Wong, T. Y., & Wake, M. A. (2019) · BMJ Open · doi:10.1136/bmjopen-2018-022399 · Cited by 17
Heritability of ambulatory and office blood pressure in the Swiss population
Alwan, H., Ehret, G., Ponte, B., Pruijm, M. T., Ackermann, D., Guessous, I., Staessen, J. A., Asayama, K., Kutalik, Z., Vuistiner, P., et al. (2015) · Journal of Hypertension · doi:10.1097/hjh.0000000000000681 · Cited by 17
Affective enhancement of working memory is maintained in depression.
Schweizer, S., Navrady, L. B., Breakwell, L., Howard, R. M., Golden, A.-M. J., Werner‐Seidler, A., & Dalgleish, T. (2017) · Emotion · doi:10.1037/emo0000306 · Cited by 17
Bishop, D., & Bates, T. C. (2020) · Wellcome Open Research · doi:10.12688/wellcomeopenres.15524.2 · Cited by 16
‘There and Back Again’—Forward Genetics and Reverse Phenotyping in Pulmonary Arterial Hypertension
Swietlik, E. M., Prapa, M., Martin, J. M., Pandya, D., Auckland, K., Morrell, N. W., & Gräf, S. (2020) · Genes · doi:10.3390/genes11121408 · Cited by 15
Dissecting the heritable risk of breast cancer: From statistical methods to susceptibility genes
Fanfani, V., Zátopková, M., Harris, A. L., Pezzella, F., & Stracquadanio, G. (2020) · Seminars in Cancer Biology · doi:10.1016/j.semcancer.2020.06.001 · Cited by 15
Why are education, socioeconomic position and intelligence genetically correlated?Preprint
Morris, T., Davies, N. M., Hemani, G., & Smith, G. D. (2019) · bioRxiv (Cold Spring Harbor Laboratory) · doi:10.1101/630426 · Cited by 16
Kurbasic, A., Poveda, A., Chen, Y., Ågren, Å., Engberg, E., Hu, F. B., Johansson, I., Barroso, I., Brändström, A., Hallmans, G., et al. (2014) · Current Nutrition Reports · doi:10.1007/s13668-014-0100-8 · Cited by 16
Wallis, D. J., Truong, L., Du, J. K. L., Tanguay, R. L., & Reif, D. M. (2021) · Toxics · doi:10.3390/toxics9040077 · Cited by 16
Heritability of dental arches and occlusal characteristics: a systematic review and meta-analysis
Giri, J., Bockmann, M. R., Brook, A. H., Farook, T. H., Meade, M. J., & Hughes, T. E. (2023) · European Journal of Orthodontics · doi:10.1093/ejo/cjad061 · Cited by 15
No large-effect low-frequency coding variation found for myocardial infarction
Holmen, O. L., Zhang, H., Zhou, W., Schmidt, E. M., Hovelson, D. H., Langhammer, A., Løchen, M., Ganesh, S. K., Mathiesen, E. B., VATTEN, L. J., et al. (2014) · Human Molecular Genetics · doi:10.1093/hmg/ddu175 · Cited by 14
Nazarian, A., & Gezan, S. A. (2015) · Journal of Heredity · doi:10.1093/jhered/esv096 · Cited by 14
Genome-Wide Association Analysis of Single-Breath D l CO
Sakornsakolpat, P., McCormack, M. C., Bakke, P. S., Gulsvik, A., Make, B. J., Crapo, J. D., Cho, M. H., & Silverman, E. K. (2019) · American Journal of Respiratory Cell and Molecular Biology · doi:10.1165/rcmb.2018-0384oc · Cited by 16
Zöller, B., Pirouzifard, M., Svensson, P. J., Holmquist, B., Stenman, E., Elston, R. C., Song, Y. E., Sundquist, J., & Sundquist, K. (2021) · Journal of the American Heart Association · doi:10.1161/jaha.120.020323 · Cited by 13
Wang, L., Wu, M., Wu, Y., Zhang, X., Li, S., He, M. X., Zhang, F., Wang, Y., & Li, J. (2022) · Computational Biology and Chemistry · doi:10.1016/j.compbiolchem.2022.107639 · Cited by 13
Systems Genetics as a Tool to Identify Master Genetic Regulators in Complex Disease
Moreno‐Moral, A., Pesce, F., Behmoaras, J. V., & Petretto, E. G. (2016) · Methods in molecular biology · doi:10.1007/978-1-4939-6427-7_16 · Cited by 12
Dissecting Motor Neuron Disease With Drosophila melanogaster
Walters, R., Manion, J., & Neely, G. G. (2019) · Frontiers in Neuroscience · doi:10.3389/fnins.2019.00331 · Cited by 12
Missing Heritability of Complex Traits and Diseases
Nolte, I. M., Tropf, F. C., & Snieder, H. (2019) · Wiley eBooks · doi:10.1002/9780470015902.a0028223 · Cited by 13
Prevalence and genetic parameters for cryptorchidism in Swedish-born Icelandic horses
Eriksson, S., Jäderkvist, K., Dalin, A., Axelsson, J., & Lindgren, G. (2015) · Livestock Science · doi:10.1016/j.livsci.2015.06.022 · Cited by 11
Damena, D., & Chimusa, E. R. (2019) · Human Molecular Genetics · doi:10.1093/hmg/ddz258 · Cited by 13
Genetics of bronchopulmonary dysplasia: When things do not match up, it is only the beginning
Bhandari, V., Gruen, J. R., Jang, K. L., Göpel, W., Hallman, M., & Lavoie, P. M. (2019) · The Journal of Pediatrics · doi:10.1016/j.jpeds.2019.01.014 · Cited by 11
Šidlauskienė, M., Papievis, V., Šidlauskas, A., Šidlauskas, M., Juzėnas, S., & Lopatienė, K. (2024) · Scientific Reports · doi:10.1038/s41598-024-70985-4 · Cited by 11
Heritability estimates on Hodgkin’s lymphoma: a genomic- versus population-based approach
Thomsen, H., Filho, M. I. D. S., Försti, A., Fuchs, M., Ponader, S., von Strandmann, E. P., Eisele, L., Herms, S., Hofmann, P., Sundquist, J., et al. (2014) · European Journal of Human Genetics · doi:10.1038/ejhg.2014.184 · Cited by 10
Schlomer, G. L., Cleveland, H. H., Feinberg, M. E., Wolf, P. S. A., Greenberg, M. T., Spoth, R. L., Redmond, C. R., Tricou, E. P., & Vandenbergh, D. J. (2016) · Child Development · doi:10.1111/cdev.12666 · Cited by 11
Heritability of haemodynamics in the ascending aorta
McGurk, K. A., Owen, B., Watson, W. D., Nethononda, R. M., Cordell, H. J., Farrall, M., Rider, O. J., Watkins, H. C., Revell, A. J., & Keavney, B. D. (2020) · Scientific Reports · doi:10.1038/s41598-020-71354-7 · Cited by 10
Advances and challenges in quantitative delineation of the genetic architecture of complex traits
Tang, H., & He, Z. (2021) · Quantitative Biology · doi:10.15302/j-qb-021-0249 · Cited by 9
Farid, M., Anshori, M. F., & Ridwan, I. (2022) · Biodiversitas Journal of Biological Diversity · doi:10.13057/biodiv/d231132 · Cited by 10
Estimating disease heritability from complex pedigrees allowing for ascertainment and covariates
Speed, D., & Evans, D. M. (2024) · The American Journal of Human Genetics · doi:10.1016/j.ajhg.2024.02.010 · Cited by 9
Westergaard, D., Jørgensen, F. H., Waaben, J., Jung, A. W., Lademann, M., Hansen, T. F., Cremers, J., Ostrowski, S. R., Pedersen, O. B., Reguant, R., et al. (2024) · Nature Communications · doi:10.1038/s41467-024-51795-8 · Cited by 12
Song, Y., & Sung, J. (2015) · Asian Journal of Andrology · doi:10.4103/1008-682x.164923 · Cited by 9
Asefa, N. G., Neustaeter, A., Jansonius, N. M., & Snieder, H. (2018) · BMJ Open · doi:10.1136/bmjopen-2017-019049 · Cited by 10
Using partitioned heritability methods to explore genetic architecture
Evans, L. M., & Keller, M. C. (2018) · Nature Reviews Genetics · doi:10.1038/nrg.2018.6 · Cited by 9
Quantifying Genetic and Environmental Influence on Gray Matter Microstructure Using Diffusion MRI
Baxi, M., Biase, M. A. D., Lyall, A. E., Karayumak, S. C., Seitz, J., Ning, L., Makris, N., Rosene, D. L., Kubicki, M. R., & Yogesh Rathi, A. (2020) · Cerebral Cortex · doi:10.1093/cercor/bhaa174 · Cited by 11
The ‘heritability’ of domestication and its functional partitioning in the pig
Miguel Pérez-enciso, A., Campos, G. D. L., Hudson, N. J., Kijas, J., & Reverter, A. (2016) · Heredity · doi:10.1038/hdy.2016.78 · Cited by 9
Liu, S., Bush, W. S., Akinyemi, R., Byrd, G. S., Caban‐Holt, A., Rajabli, F., Reitz, C., Kunkle, B. W., Tosto, G., Vance, J. M., et al. (2025) · PLoS Genetics · doi:10.1371/journal.pgen.1011701 · Cited by 9
Chromosomal characteristics of salt stress heritable gene expression in the rice genome
McGowan, M., Zhang, Z., & Ficklin, S. P. (2021) · BMC Genomic Data · doi:10.1186/s12863-021-00970-7 · Cited by 8
Tsui, N. B. Y., Cheng, G. Y.-M., Chung, T., Lam, C. W. K., Yee, A., Chung, P. K. C., Kwan, T.-K., Ko, E. Y.-L., He, D., Wong, W., et al. (2018) · Scientific Reports · doi:10.1038/s41598-017-19017-y · Cited by 8
Using genetic designs to identify likely causal environmental contributions to psychopathology
Sellers, R., Riglin, L., Harold, G. T., & Thapar, A. (2022) · Development and Psychopathology · doi:10.1017/s0954579422000906 · Cited by 8
Zhao, J., Salter‐Townshend, M., & O’Hagan, A. R. (2023) · European Actuarial Journal · doi:10.1007/s13385-023-00345-5 · Cited by 9
Fraimout, A., Guillaume, F., Li, Z., Sillanpää, M. J., Rastas, P. M. A., & Merilä, J. (2024) · Molecular Ecology · doi:10.1111/mec.17299 · Cited by 7
Franceschini, N., Haack, K., Göring, H. H. H., Voruganti, V. S., Laston, S., Almasy, L. A., Lee, E. T., Best, L. G., Fabsitz, R. R., North, K. E., et al. (2013) · Diabetologia · doi:10.1007/s00125-013-2988-8 · Cited by 8
Identifying Cancer genes by combining two-rounds RWR based on multiple biological data
Zhang, W., Lei, X., & Bian, C. (2019) · BMC Bioinformatics · doi:10.1186/s12859-019-3123-8 · Cited by 8
Yang, G., Xie, W., Li, B., Zhao, G., Li, J., Xiao, W., & Li, Y. (2024) · Aging Cell · doi:10.1111/acel.14252 · Cited by 7
Nazarian, A., & Kulminski, A. M. (2019) · Journal of Alzheimer s Disease · doi:10.3233/jad-190168 · Cited by 7
Protein misfolding in endoplasmic reticulum stress with applications to renal diseases
Nademi, S., & Dickhout, J. G. (2019) · Advances in protein chemistry and structural biology · doi:10.1016/bs.apcsb.2019.08.001 · Cited by 7
Barden, M., Anagnostopoulos, A., Griffiths, B. E., Bedford, C., Winters, M., Li, B., Coffey, M. P., Psifidi, A., Banos, G., & Oikonomou, G. (2022) · Veterinary Record · doi:10.1002/vetr.1632 · Cited by 7
The Dead Ends of Sociogenomics
Robette, N., & Reeve, P. (2022) · Population (English Edition) · doi:10.3917/popu.2202.0191 · Cited by 7
Garner, J. P., Talbot, C. F., Rosso, L. A. D., McCowan, B., Kanthaswamy, S., Haig, D., Capitanio, J. P., & Parker, K. J. (2023) · Molecular Autism · doi:10.1186/s13229-023-00556-3 · Cited by 7
O’Brien, E. K., Hunt, J., & Wolf, J. B. (2015) · Oxford University Press eBooks · doi:10.1093/obo/9780199941728-0064 · Cited by 7
McGuire, D., Markus, H., Yang, L., Xu, J., Montgomery, A., Berg, A. S., Li, Q., Carrel, L., Liu, D. J., & Jiang, B. (2024) · Nature Communications · doi:10.1038/s41467-024-49566-6 · Cited by 6
Bishop, D., & Bates, T. C. (2019) · Wellcome Open Research · doi:10.12688/wellcomeopenres.15524.1 · Cited by 6
Germline mechanisms of immunotherapy toxicities in the era of genome‐wide association studies
Gusev, A. (2023) · Immunological Reviews · doi:10.1111/imr.13253 · Cited by 7
Heritabilities of Intraocular Pressure in the Population of Korea
Kim, N. R., Park, H. J., Suh, Y. J., Chin, H. S., & Kim, C. Y. (2014) · JAMA Ophthalmology · doi:10.1001/jamaophthalmol.2013.7612 · Cited by 6
The contribution of Neanderthal introgression and natural selection to neurodegenerative diseases
Chen, Z., Reynolds, R. H., Pardiñas, A. F., Taliun, S. A. G., van Rheenen, W., Lin, K., Shatunov, A., Gustavsson, E. K., Fogh, I., Jones, A. R., et al. (2023) · Neurobiology of Disease · doi:10.1016/j.nbd.2023.106082 · Cited by 7
Heritability estimation in case-control studies
Bonnet, A. (2018) · Electronic Journal of Statistics · doi:10.1214/18-ejs1424 · Cited by 6
Genetic Regulation of Immunoglobulin G Glycosylation
Frkatović-Hodžić, A., Zaytseva, O. O., & Klarić, L. (2021) · Experientia supplementum · doi:10.1007/978-3-030-76912-3_8 · Cited by 6
Mendelian Randomization and Infection: Pitfalls and Promises
Hamilton, F., Butler‐Laporte, G., & Smith, G. D. (2025) · The Journal of Infectious Diseases · doi:10.1093/infdis/jiaf251 · Cited by 5
Environmental effects on brain functional networks in a juvenile twin population
Tassi, E., Maggioni, E., Mauri, M., Fagnani, C., Agarwal, N., Bianchi, A. M., Stazi, M. A., Nobile, M., & Brambilla, P. (2023) · Scientific Reports · doi:10.1038/s41598-023-30672-2 · Cited by 6
Influence of genetic and environmental factors on transverse growth
Al-Obaidi, S., Papageorgiou, S. N., Saade, M., Caradonna, K. M., Kantarcı, A., Will, L. A., & Motro, M. (2025) · European Journal of Orthodontics · doi:10.1093/ejo/cjaf003 · Cited by 5
Direct additive genetics and maternal effect contribute to the risk of Tourette disorder
Mahjani, B., Klei, L., Grice, A. B., Larsson, H., Hultman, C. M., Sandin, S., Devlin, B., Buxbaum, J. D., & Grice, D. E. (2023) · Journal of Neurology Neurosurgery & Psychiatry · doi:10.1136/jnnp-2022-330239 · Cited by 5
Srivastava, A. K., Juodakis, J., Solé-Navais, P., Chen, J., Bačelis, J., Teramo, K. A., Hallman, M., Njølstad, P. R., Evans, D. M., Jacobsson, B., et al. (2025) · PLoS Genetics · doi:10.1371/journal.pgen.1011575 · Cited by 5
Grassi, M. A., Rao, V. R., Winkler, K. P., Zhang, W., Bogaard, J. D., Chen, S., LaCroix, B. L., Lenkala, D., Rehman, J., Malik, A. B., et al. (2014) · PLoS ONE · doi:10.1371/journal.pone.0087883 · Cited by 5
Wolf, H. M., Romero, R. J., Strauss, J. F., Hassan, S. S., Latendresse, S. J., Webb, B. T., Tarca, A. L., Gomez‐Lopez, N., Hsu, C., & York, T. P. (2022) · BMJ Open · doi:10.1136/bmjopen-2021-053631 · Cited by 5
A Behavior Genetic Analysis of Pleasant Events, Depressive Symptoms, and Their Covariation
Whisman, M. A., Johnson, D. P., & Rhee, S. H. (2014) · Clinical Psychological Science · doi:10.1177/2167702613512793 · Cited by 6
Genetics of Brain Aging – Twin Aging
Reynolds, C. A., & Phillips, D. (2014) · Elsevier eBooks · doi:10.1016/b978-0-12-801238-3.04608-0 · Cited by 7
Detecting the dominance component of heritability in isolated and outbred human populations
Herzig, A. F., Nutile, T., Ruggiero, D., Ciullo, M., Perdry, H., & Leutenegger, A. (2018) · Scientific Reports · doi:10.1038/s41598-018-36050-7 · Cited by 6
Mahjani, B., Kępińska, A. P., Smout, S., Cohen, L., Caballero, M., Buxbaum, J. D., & Grice, D. E. (2025) · American Journal of Psychiatry · doi:10.1176/appi.ajp.20230383 · Cited by 4
Surgically Treated Degenerative Lumbar Spine Diseases in Twins
Szigethy, L., Sigmundsson, F. G., & Joelson, A. (2024) · Journal of Bone and Joint Surgery · doi:10.2106/jbjs.23.00902 · Cited by 4
Prediction of genetic contributions to complex traits using whole genome sequencing data
Yao, C., Leng, N., WEIGEL, K. A., Lee, K. E., Engelman, C. D., & Meyers, K. J. (2014) · BMC Proceedings · doi:10.1186/1753-6561-8-s1-s68 · Cited by 4
Genetic and Environmental Contributions to the Covariation Between Cardiometabolic Traits
Chen, X., Kuja‐Halkola, R., Chang, Z., Karlsson, R., Hägg, S., Svensson, P., Pedersen, N. L., & Magnusson, P. K. E. (2018) · Journal of the American Heart Association · doi:10.1161/jaha.117.007806 · Cited by 5
Inherited dreams: A twin study of future orientation and heritability among chinese adolescents
Zheng, L., Chen, J., Li, X., & Gan, Y. (2021) · European Journal of Developmental Psychology · doi:10.1080/17405629.2021.1889504 · Cited by 4
What Have We Learned From Family-Based Studies About Spondyloarthritis?
Costantino, F., Mambueni, H. M., Said‐Nahal, R., Garchon, H., & Bréban, M. (2021) · Frontiers in Genetics · doi:10.3389/fgene.2021.671306 · Cited by 4
Cohort profile and heritability assessment of familial pancreatic cancer: a nation-wide study
Tan, M., Brusgaard, K., Gerdes, A., Mortensen, M. B., Detlefsen, S., de Muckadell, O. B. S., & Jøergensen, M. T. (2021) · Scandinavian Journal of Gastroenterology · doi:10.1080/00365521.2021.1937697 · Cited by 4
Chozas, A. C., Mahjani, B., & Rönnegård, L. (2021) · Human Heredity · doi:10.1159/000521215 · Cited by 4
Variational bayesian method of estimating variance components
Arakawa, A., Taniguchi, M., Hayashi, T., & Mikawa, S. (2016) · Animal Science Journal · doi:10.1111/asj.12514 · Cited by 4
Mularo, A. J., Bernal, X. E., & DeWoody, J. A. (2022) · Journal of Heredity · doi:10.1093/jhered/esac007 · Cited by 4
Polubriaginof, F. C. G., Vanguri, R., Quinnies, K., Belbin, G. M., Yahi, A., Salmasian, H., Lorberbaum, T., Nwankwo, V., Li, L., Shervey, M., et al. (2018) · SSRN Electronic Journal · doi:10.1101/066068 · Cited by 4
Schiavon, M., Burton, B. K., Hemager, N., Greve, A. N., Spang, K. S., Ellersgaard, D., Plessen, K. J., Jepsen, J. R. M., Thorup, A. A. E., Werge, T. M., et al. (2025) · European Journal of Neuroscience · doi:10.1111/ejn.70163 · Cited by 3
Fast heritability estimation based on MINQUE and batch training
Tang, M., Hou, T., Tong, X., Shen, X., Zhang, X., Wang, T., & Lu, Q. L. (2022) · Briefings in Bioinformatics · doi:10.1093/bib/bbac115 · Cited by 3
Integrating multi-layered biological priors to improve genomic prediction accuracy in beef cattle
Zhao, Z., Niu, Q., Wu, J., Wu, T., Xie, X., Wang, Z., Zhang, L., Gao, H., Gao, X. J., Xu, L., et al. (2024) · Biology Direct · doi:10.1186/s13062-024-00574-y · Cited by 4
Yuan, M., Goovaerts, S., Lee, M. K., Devine, J., Richmond, S., Walsh, S., Shriver, M. D., Shaffer, J. R., Marazita, M. L., Peeters, H., et al. (2025) · Briefings in Bioinformatics · doi:10.1093/bib/bbaf090 · Cited by 3
Baker, S. G. (2016) · Biometrics · doi:10.1111/biom.12460 · Cited by 3
Molecular Biomarkers of Health
Nehlin, J. O., & Andersen, O. (2020) · Healthy ageing and longevity · doi:10.1007/978-3-030-52663-4_15 · Cited by 3
Does persistence to methotrexate treatment in early rheumatoid arthritis have a familial component?
Sysojev, A. Ö., Frisell, T., Delcoigne, B., Saevarsdóttir, S., Askling, J., & Westerlind, H. (2022) · Arthritis Research & Therapy · doi:10.1186/s13075-022-02873-z · Cited by 3
Muneeb, M., Feng, S. F., & Henschel, A. (2022) · International Conference on Bioinformatics and Biomedical Technology (ICBBT) · doi:10.1145/3543377.3543387 · Cited by 3
Yuan, Y., Zhou, M. R., Li, Z., Jiang, D. L., Wang, Z., & Fang, M. (2025) · Aquaculture · doi:10.1016/j.aquaculture.2024.742114 · Cited by 3
Familial liability to schizophrenia and mood disorders and cognitive impairment in psychosis
Cuesta, M. J., Zarzuela, A., Sánchez-Torres, A. M., Lorente-Omeñaca, R., Moreno-Izco, L., Sanjuán, J., & Peralta, V. (2015) · Psychiatry Research · doi:10.1016/j.psychres.2015.03.024 · Cited by 3
Clinical Multigene Testing for Prostate Cancer
Berro, T., Barrett, E., & AlDubayan, S. H. (2021) · Urologic Clinics of North America · doi:10.1016/j.ucl.2021.03.002 · Cited by 3
Multidimensional Heritability Analysis of Neuroanatomical ShapePreprint
Ge, T., Reuter, M., Winkler, A. M., Holmes, A. J., Lee, P. H., Tirrell, L. S., Roffman, J. L., Buckner, R. L., Smoller, J. W., & Sabuncu, M. R. (2015) · bioRxiv (Cold Spring Harbor Laboratory) · doi:10.1101/033407 · Cited by 3
Metadata
- Authors
- Tenesa, A., & Haley, C. S.
- Affiliations
- Roslin Institute (GB)
- Corresponding author
- Tenesa, Albert
- Venue
- Nature Reviews Genetics
- Published
- 2013-01-18
- Volume
- 14
- Issue
- 2
- Pages
- 139-149
- ISSN
- 1471-0056 (ISSN-L)
- 1471-0064
- OpenAlex
- W2040924786
- Cited by
- 283
- References
- 90
- Citations by year
- 2026: 10 · 2025: 13 · 2024: 13 · 2023: 15 · 2022: 20 · 2021: 24 · 2020: 22 · 2019: 30 · 2018: 35 · 2017: 20 · 2016: 23 · 2015: 27 · 2014: 22 · 2013: 9
- FWCI
- 3.27
- Type
- journal article
- Language
- en
- Open access
- closed
- Licence
- www.springer.com/tdm (tdm)
- Locations
- Nature Reviews Genetics (publishedVersion)
- PubMed (publishedVersion)
- Funders
- Cancer Research UK (C12229/A13154, 13154)
- Medical Research Council
- Biotechnology and Biological Sciences Research Council (BBS/E/D/20211553, BB/K000195/1)
- Topics
- Life Sciences › Biochemistry, Genetics and Molecular Biology › Genetics › Genetic Associations and Epidemiology
- Life Sciences › Biochemistry, Genetics and Molecular Biology › Genetics › Genetic and phenotypic traits in livestock
- Life Sciences › Biochemistry, Genetics and Molecular Biology › Genetics › Genomics and Rare Diseases
- Keywords
- heritability, human disease, heritability estimation, genetic and environmental contributions, phenotypic variance, familial aggregation, relatives
- MeSH terms
- Disease, Environment, Female, Humans, Male, Models, Genetic, Pedigree, Models, Statistical, Bias, Linear Models, Twin Studies as Topic, Genetic Predisposition to Disease, Genetic Association Studies
About these checks
Registry, retraction, Cites and statistics results are computed, not judged, with one exception: a printed reference that no index lists is read once by a model before it counts as a citation error. Claims are extracted by a model and kept only when their quote appears verbatim in the text; each cited source is then checked, with a model’s help, for whether it says what the claim relies on. Those verdicts can be wrong — read the claim’s quote and the cited source before relying on one.
Statistics and arithmetic are recomputed, not judged.
Confidence bands are shown only for fields calibrated on our annotated test set. None is calibrated yet, so no band is shown.
What counts as a claim ›How we measure confidence ›How we check this ›
Are you an author, or do you see a problem with this page? Request a review